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Converting a DNA Damage Checkpoint Effector (UmuD2C) into a Lesion Bypass Polymerase (UmuD'2C)
Authors
Ferentz, A.E., Walker, G.C., Wagner, G.
Assembly
UMUD PROTEIN
Entity
1. UMUD PROTEIN (polymer, Thiol state: not present), 115 monomers, 12298.90 × 2 Da Detail

AFPSPAADYV EQRIDLNQLL IQHPSATYFV KASGDSMIDG GISDGDLLIV DSAITASHGD IVIAAVDGEF TVKKLQLRPT VQLIPMNSAY SPITISSEDT LDVFGVVIHV VKAMR


Total weight
24597.8 Da
Max. entity weight
12298.9 Da
Source organism
Escherichia coli
Exptl. method
NMR
Refine. method
simulated annealing
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 98.3 %, Completeness: 68.8 %, Completeness (bb): 79.9 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All68.8 % (880 of 1280)72.2 % (470 of 651)59.1 % (303 of 513)92.2 % (107 of 116)
Backbone79.9 % (542 of 678)96.1 % (222 of 231)63.0 % (213 of 338)98.2 % (107 of 109)
Sidechain61.3 % (435 of 710)59.0 % (248 of 420)66.1 % (187 of 283) 0.0 % (0 of 7)
Aromatic21.1 % (16 of 76)42.1 % (16 of 38) 0.0 % (0 of 38)
Methyl81.9 % (136 of 166)84.3 % (70 of 83)79.5 % (66 of 83)

1. UMUD PROTEIN

AFPSPAADYV EQRIDLNQLL IQHPSATYFV KASGDSMIDG GISDGDLLIV DSAITASHGD IVIAAVDGEF TVKKLQLRPT VQLIPMNSAY SPITISSEDT LDVFGVVIHV VKAMR

Sample #1

Pressure 1 atm, Temperature 303 K, pH 6.0


#NameIsotope labelingTypeConcentration
1UMUD PROTEIN[U-15N]0.9 mM
2NaCl150 mM
3phosphate10 mM
4DTT1 mM
5EDTA0.1 mM
6H2O95 %
7D2O5 %
Sample #2

Pressure 1 atm, Temperature 303 K, pH 6.0


#NameIsotope labelingTypeConcentration
8UMUD PROTEIN[U-15N; U-13C]1.3 mM
9NaCl150 mM
10phosphate20 mM
11DTT1 mM
12EDTA0.1 mM
13H2O95 %
14D2O5 %

Protein Blocks Logo
Calculated from 20 models in PDB: 1I4V, Strand ID: A, B Detail


Release date
2003-01-06
Citation
Converting a DNA damage checkpoint effector (UmuD2C) into a lesion bypass polymerase (UmuD'2C)
Ferentz, A.E., Walker, G.C., Wagner, G.
EMBO J. (2001), 20, 4287-4298, PubMed 11483531 , DOI 10.1093/emboj/20.15.4287 ,
Related entities 1. UMUD PROTEIN, : 1 : 5 : 79 entities Detail
Experiments performed 4 experiments Detail
nullKeywords SOS response, SOS mutagenesis, DNA repair, DNA polymerase V, DNA polymerase accessory protein, LexA repressor, lambda CI, signal peptidase, serine-lysine dyad, autocatalytic cleavage, serine protease